FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

HYTEC AUTOIMMUNE KITS (SM)

K Number: K954896 · Decision Mar 22, 1996
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
27
Applicant Total
51
Review Days
185

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Basic Information

Device Name
HYTEC AUTOIMMUNE KITS (SM)
K Number
K954896
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hycor Biomedical, Inc.
Date Received
September 19, 1995
Decision Date
March 22, 1996
Product Code
LKP
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LKP Anti-Sm Antibody, Antigen And Control

Similar 510(k) Clearances

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Other Clearances by Hycor Biomedical, Inc.

K Number Device Name
K081217 HY-TEC SPECIFIC AND TOTAL IGE EIA SYSTEM
K080322 HY*TEC EXTENDED SPECIFIC IGE EIA, MCS ASSAY USING TECAN FREEDOM EVO RSP 200
K022944 AUTOSTAT II ANTI-B-2 GLYCOPROTEIN-I IGM ELISA
K022945 AUTOSTAT II ANTI-B-2 GLYCOPROTEIN I IGG ELISA
K965094 HYCOR ALLERGEN DISC
K962730 HYCOR HY.TEC/MANUAL DS-DNA AUTO-ANTIBODY
K962720 HYCOR HY.TEC/MANUAL SCL-70 AUTO-ANTIBODY
K962729 HYCOR HY.TEC/MANUAL RF AUTO-ANTIBODY
K962578 HYCOR HY.TEC/MANUAL SS-B AUTO-ANTIBODY
K962722 HYCOR HY.TEC/MANUAL SM AUTO-ANTIBODY
Search all 51 clearances from Hycor Biomedical, Inc. →